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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

MPR10-06BAS-00 — Class IIa MDR by Medical Products Research

MD Atlas
Medical Products Research

EUDAMED last updated this device on Oct 13, 2025

MPR10-06BAS-00

805709490NMTXXAAA00WC

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medical Products Research
UDI-DI code: 08057094902033
Reference / catalog number: MPR10-06BAS-00

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View device family (Basic UDI)

Manufacturer information

Organization name: Medical Products Research
SRN: IT-MF-000025583
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08057094902033
Basic UDI-DI: 805709490NMTXXAAA00WC
Reference / catalog number: MPR10-06BAS-00
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The device is sold with the starter kit in a cardboard. The assembly is identified with a different UDI-DI.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08057094902033

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12159009EQUIPMENT FOR REMOVAL OF SECRETIONS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Related devices

MPR10-05BAS-00805709490NMTXXAAA00WCOn the market MPR10-05COM-00805709490NMTXXAAA00WCOn the market MPR10-05PRO-00805709490NMTXXAAA00WCOn the market MPR10-05SAT-00805709490NMTXXAAA00WCOn the market MPR40-01-00805709490FAHXX00MEOn the market

Certificates

Certificate health across this manufacturer's portfolio.

0425-MDR-030143-00Issued
Quality management systemNotified body: 0425Expiry: Aug 4, 2030
0425-MDR-030128-00Issued
Quality management systemNotified body: 0425Expiry: Mar 13, 2030